NDC codes

FDA NDC Directory
Product NDC (as listed)48433-141Labeler and product segments. Claims need a package NDC.
Product NDC at billing width48433-0141Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
48433-141-2048433014120100 BLISTER PACK in 1 CARTON (48433-141-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-141-01)Marketed from Apr 7, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Trifluoperazine Hydrochloride
Generic name (nonproprietary)
trifluoperazine hydrochloride
Active ingredients
Trifluoperazine hydrochloride — 2 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040209
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 48433-141_51015912-4104-ed2c-e063-6294a90ab288SPL ID 51015912-4104-ed2c-e063-6294a90ab288SPL set ID 8501543b-0c74-4087-9946-e7198400814aRxCUI 198322, 198323, 198324, 198325UNII 6P1Y2SNF5V
Pharmacologic class
Phenothiazine

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N448433014120 followed by a unit qualifier and the quantity

Package 48433-0141-20. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE For the management of schizophrenia. Trifluoperazine hydrochloride tablets, USP are effective for the short-term treatment of generalized non-psychotic anxiety. However, trifluoperazine hydrochloride tablets are not the first drug to be used in therapy for most patients with non-psychotic anxiety because certain risks associated with its use are not shared by common alternative treatments (i.e., benzodiazepines). When used in the treatment of non-psychotic anxiety, trifluoperazine hydrochloride tablets should not be administered at doses of more than 6 mg per day or for longer than 12 weeks because the use of trifluoperazine hydrochloride tablets at higher doses or for …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040209

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 040209
ProductStrengthForm · routeLabelerProduct NDC
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 1 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-572
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 2 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-573
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 5 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-574
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 10 mg/1Tablet, Film coatedOralMylan Institutional Inc.51079-575
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 10 mg/1Tablet, Film coatedOralSafecor Health LLC48433-143
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 1 mg/1Tablet, Film coatedOralSafecor Health LLC48433-140
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 5 mg/1Tablet, Film coatedOralSafecor Health LLC48433-142
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 1 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-2401
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 2 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-2402
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 2 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2095
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 5 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2106
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 5 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-2405
Trifluoperazine HydrochlorideTrifluoperazine hydrochloride 10 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-2410

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Trifluoperazine Hydrochloride NDC 48433-141 | Med-Code